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角蛋白微颗粒的特性研究:羽毛生物质具有强大的抗氧化和抗癌活性。

Characterization of keratin microparticles from feather biomass with potent antioxidant and anticancer activities.

机构信息

Faculty of Chemical Engineering and Natural Resources, Universiti Malaysia Pahang, Lebuhraya Tun Razak, 26300 Gambang, Pahang, Malaysia.

Faculty of Chemical Engineering and Natural Resources, Universiti Malaysia Pahang, Lebuhraya Tun Razak, 26300 Gambang, Pahang, Malaysia.

出版信息

Int J Biol Macromol. 2017 Nov;104(Pt A):189-196. doi: 10.1016/j.ijbiomac.2017.06.015. Epub 2017 Jun 10.

DOI:10.1016/j.ijbiomac.2017.06.015
PMID:28596005
Abstract

In the present study chicken feathers were hydrolyzed by chemical treatment in alkaline conditions. The pH value of feather hydrolyzed solution was amended accordingly the iso-electric precipitation. Two types of keratin microparticles KM1, KM2 were synthesized under acidic conditions at 3.5 and 5.5pH respectively. The synthesized keratin microparticles possessed uniform and round surface by scanning electron microscopy (SEM). The thermal degradation of microparticles were examined by thermogravimetry (TGA). Fourier transform infrared spectroscopy (FTIR) revealed that the extracted keratin retained the most of protein backbone. The microparticles were screened for their in vitro anticancer activities by SRB bioassay towards HeLa, SK-OV-3 and A549 cancer cell lines. Futhermore, their cytotoxicity towards healthy cell lines was analyzed having Malin Darby canine kidney (MDCK) cell lines along with in vitro antioxidant activity using DPPH and ABTS methods KM1 and KM2 showed 200.31±1.01 and 139.73±0.94, 214.16±0.29 and 153.92±0.61, 328.92±3.46 and 200.33±2.48μg/mL of IC levels against HeLa, SK-OV-3, and A549 cell lines, respectively. Moreover, KM1 and KM2 demonstrated significant antioxidant potency with IC levels 13.15 and 9.02μg/mL as well as 8.96 and 5.60μg/mL in DPPH and ABTS radical scavenging bioassay, respectively.

摘要

在本研究中,鸡羽毛通过化学处理在碱性条件下进行水解。根据等电沉淀,相应地调整羽毛水解溶液的 pH 值。在 3.5 和 5.5 pH 下分别在酸性条件下合成了两种类型的角蛋白微球 KM1、KM2。扫描电子显微镜 (SEM) 显示合成的角蛋白微球具有均匀且圆形的表面。通过热重分析 (TGA) 检查微球的热降解。傅里叶变换红外光谱 (FTIR) 表明提取的角蛋白保留了大部分蛋白质骨架。通过 SRB 生物测定法,对角质微粒的体外抗癌活性进行了筛选,针对 HeLa、SK-OV-3 和 A549 癌细胞系。此外,还通过 MDCK 细胞系分析了它们对健康细胞系的细胞毒性,并通过 DPPH 和 ABTS 方法分析了体外抗氧化活性。KM1 和 KM2 对 HeLa、SK-OV-3 和 A549 细胞系的 IC 水平分别为 200.31±1.01 和 139.73±0.94、214.16±0.29 和 153.92±0.61、328.92±3.46 和 200.33±2.48μg/mL。此外,KM1 和 KM2 表现出显著的抗氧化能力,IC 水平分别为 13.15 和 9.02μg/mL 以及 DPPH 和 ABTS 自由基清除生物测定中的 8.96 和 5.60μg/mL。

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